For Sponsors & CROs

MCR eSource Remote
Viewer™ (eSRV™)

For clinical trials sponsors and CROs companies

What is MCR eSource Remote Viewer™ ?

MCR eSource Remote Viewer™ (eSRV™) is a remote study monitoring system in a hybrid model. 

It is one of three systems developed by MCR Clinic™ for clinical trials. 

These systems do – at any stage – interfere with existing hospitals or clinical research study systems. What is more, they are designed to work in the background and integrate seamlessly.


All MCR Clinic™ systems share the same communication module with dynamically generated forms, allowing site, sponsor, CRO and technical support staff to efficiently contact and notify each other.

Most study or subject information and data is automatically generated or appended to messages, speeding communication, making it user-friendly, error-free and adding another layer of data security.

Benefits for Monitor and Sponsor

MCR eSource Remote Viewer™ (eSRV™) provides remote access to eSource

Savings

Estimated 25% reduction in monitoring costs by replacing some face-to-face visits with remote access to data.

Security

Only authorized individuals have access to data, no more “over the shoulder” access.

Speed

Remote access to data updated every 24 hours with the ability to review and edit at any time.

Monitoring

Reduce visits by physical monitors in favor of remote access to eSource in #modelhybrid.

Efficiency

Minimizes the possibility of errors  generating statistically healthier data.

 

Automation

Minimize manual data verification  automate eSource data verification.

Other MCR CLINIC™ Systems

MCR Clinical Site Manager™ (CSM™)

System for site managers and study coordinators to effectively contract, supervise and bill.

MCR Data Communication Integrator™ (DCI™)

System for secure and automatic data exchange between different systems used in clinical trials.

MCR Clinic™ systems security

Tested in a real-world environment

MCR Clinic™ systems have been tested in oncology studies conducted at university hospitals, in cooperation with leading pharmaceutical companies.

Compliant with national and international standards

MCR Clinic™ systems are designed to operate in accordance with the Regulatory Model based on regulations and guidelines for both clinical trials, data protection and health care information system.

Meet the highest IT requirements

MCR Clinic™ systems meet the highest requirements for medical IT in Cloud and Software-as-a-Service infrastructure (Microsoft Azure, FHIR Fast Healthcare Interoperable Resource, HL7 CDA and higher for medical data storage and exchange).

Email or call to schedule an appointment

Krystyna Antolak

+48 789 229 070

k.antolak@mcr.clinic

Anna Urban-Marcinkiewicz

   +48 789 266 610    

a.marcinkiewicz@mcr.clinic